Serum protein profiling and proteomics in autistic spectrum disorder using magnetic bead-assisted mass spectrometry

被引:44
作者
Taurines, Regina [1 ]
Dudley, Edward [2 ]
Conner, Alexander C. [1 ]
Grassl, Julia [1 ]
Jans, Thomas [3 ]
Guderian, Frank [3 ]
Mehler-Wex, Claudia [4 ]
Warnke, Andreas [3 ]
Gerlach, Manfred [3 ]
Thome, Johannes [1 ]
机构
[1] Swansea Univ, Sch Med, Inst Life Sci, Acad Unit Psychiat, Swansea SA2 8PP, W Glam, Wales
[2] Swansea Univ, SOTEAS, Biochem Res Grp, Swansea SA2 8PP, W Glam, Wales
[3] Univ Wurzburg, Dept Child & Adolescent Psychiat & Psychotherapy, Wurzburg, Germany
[4] Univ Ulm, Dept Child & Adolescent Psychiat & Psychotherapy, Ulm, Germany
关键词
Autism; Biomarker discovery; Serum profiling; Proteomics; INFANTILE-AUTISM; SEROTONIN TRANSPORTER; MENTAL-RETARDATION; NEONATAL BLOOD; CHILDREN; CANCER; NOREPINEPHRINE; NEUROTROPHINS; NEUROPEPTIDES; MARKERS;
D O I
10.1007/s00406-009-0066-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The pathophysiology of autistic spectrum disorder (ASD) is not fully understood and there are no diagnostic or predictive biomarkers. Proteomic profiling has been used in the past for biomarker research in several non-psychiatric and psychiatric disorders and could provide new insights, potentially presenting a useful tool for generating such biomarkers in autism. Serum protein pre-fractionation with C8-magnetic beads and protein profiling by matrix-assisted laser desorption/ionisation-time of flight-mass spectrometry (MALDI-ToF-MS) were used to identify possible differences in protein profiles in patients and controls. Serum was obtained from 16 patients (aged 8-18) and age-matched controls. Three peaks in the MALDI-ToF-MS significantly differentiated the ASD sample from the control group. Sub-grouping the ASD patients into children with and without comorbid Attention Deficit and Hyperactivity Disorder, ADHD (ASD/ADHD+ patients, n = 9; ASD/ADHD- patients, n = 7), one peak distinguished the ASD/ADHD+ patients from controls and ASD/ADHD- patients. Our results suggest that altered protein levels in peripheral blood of patients with ASD might represent useful biomarkers for this devastating psychiatric disorder.
引用
收藏
页码:249 / 255
页数:7
相关论文
共 45 条
[1]   BEHAVIORAL-PROBLEMS AND COMPETENCIES REPORTED BY PARENTS OF NORMAL AND DISTURBED-CHILDREN AGED 4 THROUGH 16 [J].
ACHENBACH, TM ;
EDELBROCK, CS .
MONOGRAPHS OF THE SOCIETY FOR RESEARCH IN CHILD DEVELOPMENT, 1981, 46 (01) :1-82
[2]  
[Anonymous], 1999, HAMBURG WECHSLER INT
[3]  
[Anonymous], ADOS DIAGNOSTISCHE B
[4]   Autism as a disorder of neural information processing: directions for research and targets for therapy [J].
Belmonte, MK ;
Cook, EH ;
Anderson, GM ;
Rubenstein, JLR ;
Greenough, WT ;
Beckel-Mitchener, A ;
Courchesne, E ;
Boulanger, LM ;
Powell, SB ;
Levitt, PR ;
Perry, EK ;
Jiang, YH ;
DeLorey, TM ;
Tierney, E .
MOLECULAR PSYCHIATRY, 2004, 9 (07) :646-663
[5]  
BOELTE S, 2006, PF FSK FRAGEBOGEN SO
[6]  
BOELTE SRD, 2006, ADI R DIAGNOSTICHES
[7]   Oral cancer plasma tumor marker identified with bead-based affinity-fractionated proteomic technology [J].
Cheng, AJ ;
Chen, LC ;
Chien, KY ;
Chen, YJ ;
Chang, JTC ;
Wang, HM ;
Liao, CT ;
Chen, IH .
CLINICAL CHEMISTRY, 2005, 51 (12) :2236-2244
[8]  
Cook E H Jr, 1990, J Neuropsychiatry Clin Neurosci, V2, P268
[9]  
Cook Edwin H. Jr., 1996, Current Opinion in Pediatrics, V8, P348, DOI 10.1097/00008480-199608000-00008
[10]   A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins [J].
Corbett, B. A. ;
Kantor, A. B. ;
Schulman, H. ;
Walker, W. L. ;
Lit, L. ;
Ashwood, P. ;
Rocke, D. M. ;
Sharp, F. R. .
MOLECULAR PSYCHIATRY, 2007, 12 (03) :292-306